Stress Clinical Trial - Radicle Relaxation 24: A Study of Health &

Status Active, not recruiting

Clinical Trial Summary

A randomized, double-blind, placebo-controlled study assessing the impact of health and wellness products on stress and related health outcomes

Clinical Trial Description

This is a randomized, double-blind, placebo-controlled study conducted with adult participants, residing in the United States. Eligible participants will (1) endorse a desire for less stress (2) have the opportunity for meaningful improvement (at least 20%) in their primary health outcome, and (3) express acceptance in taking a product and not knowing its formulation until the end of the study. Participants that report a known cardiac dysfunction, liver or kidney disease may be excluded. Participants that report a known contraindication or with well-established, significant safety concerns due to illness will be excluded. Heavy drinkers and those who report they are pregnant, trying to become pregnant, or breastfeeding will be excluded. Participants that report taking medications with a known contraindication or with well-established, significant safety concerns will be excluded. Self-reported data are collected electronically from eligible participants over 7 weeks. Participant reports of health indicators will be collected during baseline, throughout the active period of study product use, and in a final survey. All study assessments will be electronic; there are no in-person visits or assessments for this real-world evidence study. ;

Study Design

Related Conditions & MeSH terms

Stress

Clinical Trial Details

NCT number	NCT06378801
Study type	Interventional
Source	Radicle Science
Contact
Status	Active, not recruiting
Phase	N/A
Start date	February 29, 2024
Completion date	November 2024

View Details

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Radicle Relaxation 24: A Study of Health and Wellness Products on Stress and Related Health Outcomes

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms